I+D, farmacovigilancia y asuntos reglamentarios

I+D, Farmacovigilancia y Regulatory Affairs

Investigar, desarrollar, probar y lanzar nuevas soluciones farmacológicas. El proceso de desarrollo dura de 8 a 10 años y consta de 4 fases.

  • I+D, Farmacovigilancia y Regulatory Affairs

    Investigar, desarrollar, probar y lanzar nuevas soluciones farmacológicas. El proceso de desarrollo dura de 8 a 10 años y consta de 4 fases.

Título Sort ascending Ubicación Fecha Req ID
Restablecer
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Cary, NC, US 20 ago 2026 7551
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Parma, IT 15 ago 2026 7394
Senior Process Scientist - gRNA process development Parma, IT 30 ago 2026 7404
Senior Process Scientist - LNP process development
Senior Process Scientist - LNP process development Europe, remote, IT 26 ago 2026 7645
Europe, remote, IT 26 ago 2026 7645
Senior Technical Leader, Analytical Method Development and Validation, GRD CMC Parma, IT 10 sept 2026 7606
Senior Technical Leader, GRD CMC
Senior Technical Leader, GRD CMC Parma, IT 10 sept 2026 7607
Parma, IT 10 sept 2026 7607
Senior Technical Leader, Protein Biologics Development, GRD CMC Parma, IT 10 sept 2026 7605
Specialist Care Therapeutic Area, Global Regulatory Affairs and Patient Safety - Temporary Paris, Bois Colombes, FR 3 sept 2026 7450
Statistical Programmer
Statistical Programmer Parma, IT 4 sept 2026 7444
Parma, IT 4 sept 2026 7444